Canonical Allele Identifier: CA1581197821

Gene: SLC12A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186797T= , CM000667.2:g.128186797T=	GRCh38
NC_000005.9:g.127522489T= , CM000667.1:g.127522489T=	GRCh37
NC_000005.8:g.127550388T=	NCBI36
NG_042286.1:g.108007T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.*166T= MANE Select	ENSP00000262461.2:n.*166T=
ENST00000262461.6:c.*166T=	ENSP00000262461.2:n.*166T=
ENST00000343225.4:c.*166T=	ENSP00000340878.4:n.*166T=
ENST00000509205.5:c.*418T=	ENSP00000427109.1:n.*418T=
NM_001046.2:c.*166T=	NP_001037.1:n.*166T=
NM_001256461.1:c.*166T=	NP_001243390.1:n.*166T=
NR_046207.1:n.4035T=
XM_017009771.1:c.*166T=	XP_016865260.1:n.*166T=
XR_001742214.1:n.4029T=
NM_001046.3:c.*166T= MANE Select	NP_001037.1:n.*166T=
NM_001256461.2:c.*166T=	NP_001243390.1:n.*166T=
NR_046207.2:n.4060T=